A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058993



Internal ID20626033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23343301..23346200hg38UCSC Ensembl
chr1:23669794..23672693hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319725
Supporting Variants
Samples
Known GenesHNRNPR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058993
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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